A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3113338



Internal ID21296604
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:80134583..80138395hg38UCSC Ensembl
Innerchr12:80528363..80532175hg19UCSC Ensembl
Cytoband12q21.31
Allele length
AssemblyAllele length
hg383813
hg193813
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14093751
Samplessample353
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3113338
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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